Biology:RASGEF1A
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Revision as of 05:40, 25 November 2021 by imported>Corlink (fix)
 Generic protein structure example |
RasGEF domain family, member 1A is a protein that in humans is encoded by the RASGEF1A gene.[1]
References
Further reading
- "Enhanced RASGEF1A expression is involved in the growth and migration of intrahepatic cholangiocarcinoma". Clinical Cancer Research 12 (22): 6611–6. Nov 2006. doi:10.1158/1078-0432.CCR-06-0783. PMID 17121879.
- "A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk". Nature 434 (7035): 857–63. Apr 2005. doi:10.1038/nature03467. PMID 15829955.
- "Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease". Proceedings of the National Academy of Sciences of the United States of America 106 (8): 2694–9. Feb 2009. doi:10.1073/pnas.0809630105. PMID 19196962.
- "RasGEF1A and RasGEF1B are guanine nucleotide exchange factors that discriminate between Rap GTP-binding proteins and mediate Rap2-specific nucleotide exchange". The FEBS Journal 276 (16): 4607–16. Aug 2009. doi:10.1111/j.1742-4658.2009.07166.x. PMID 19645719.
- "Identifying candidate Hirschsprung disease-associated RET variants". American Journal of Human Genetics 76 (5): 850–8. May 2005. doi:10.1086/429589. PMID 15759212.
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